Reacción #46133

ord-78e7680319ce4f77916ddc0d86a4e158

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe solvent was removed in vacuo
  2. 2
    workup.DISSOLUTIONthe residue was dissolved in THF and neutralized with 1N HCl
  3. 3
    OtroVolatiles were removed under vacuum
  4. 4
    Otrothe product was purified by prep-HPLC
  5. 5
    workup.ADDITIONThe fraction containing the title compound
  6. 6
    Otroevaporated
  7. 7
    workup.DISSOLUTIONThe residue was dissolved in EtOAc
  8. 8
    Lavadowashed with water
  9. 9
    Secadodried over anhydrous Na2SO4
  10. 10
    OtroThe solvent was removed under vacuum
  11. 11
    Otroto give Example 126

Procedimiento

To a solution of (S)-2-phenyl-propionic acid 2,2,2-trifluoro-1-[(S)-3-hydroxy-1-((S)-2-phenyl-propionyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-7-yl]-1-trifluoromethyl-ethyl ester (15.0 mg, 0.025 mmol), which was prepared from Example 81 by a similar procedure as that used to prepare 101A, in MeOH (0.5 mL) was added 1N NaOH (0.05 mL, 0.05 mmol) and the mixture was stirred at rt for 5 h. The solvent was removed in vacuo and the residue was dissolved in THF and neutralized with 1N HCl. Volatiles were removed under vacuum and the product was purified by prep-HPLC. The fraction containing the title compound was neutralized with 1N NaOH and evaporated. The residue was dissolved in EtOAc, washed with water, and dried over anhydrous Na2SO4. The solvent was removed under vacuum to give Example 126. LC/MS m/z 462.2 (M+H)+. 1H NMR (500 MHz, Methanol) δ 7.74 (d, 1H), 7.49 (d, 1H), 7.38 (s, 1H), 7.10 (m, 1H), 7.03 (m, 2H), 6.55 (d, 2H), 4.70 (dd, 1H), 3.91 (m, 1H), 3.59 (m, 1H), 2.36 (t, 1H), 2.07 (m, 1H), 1.89 (m, 1H), 1.35 (d, 3H), 1.31 (m, 1H), 1.12 (m, 1H).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07741317B2uspto-grants-2010_06